| Literature DB >> 27434658 |
Shabi Thankaraj Salammal1, Zhongqiang Zhang1, Jiehuan Chen1, Basab Chattopadhyay2, Jiake Wu1, Lei Fu1, Congcheng Fan1, Hongzheng Chen1.
Abstract
Four different polymorphic conformations of diethyl 5,5'-[5,5'-[2,5-bis(2-ethylhexyl)-3,6-dioxo-2,3,5,6-tetrahydropyrrolo[3,4-c]pyrrole-1,4-diyl]bis(thiophene-5,2-diyl)]difuran-2-carboxylate (DPP-(CF)2), namely, DPP-(CF)2-α, DPP-(CF)2-β, DPP-(CF)2-γ, and DPP-(CF)2-ω, were identified from X-ray diffraction analysis conducted on their thin films and single crystals. Highly crystalline and well-textured thin films of these four polymorphs were successfully prepared via postgrowth solvent vapor and thermal annealing treatments to investigate the polymorphic phase-dependent optical and electrical properties of DPP-(CF)2. Interestingly, during the phase transition from DPP-(CF)2-α to DPP-(CF)2-ω, the optical band gap decreases from 1.75 to 1.5 eV because of the enhanced π-π interaction between the neighboring molecules. Except for DPP-(CF)2-γ, the other three phases show ambipolar charge transport. Although DPP-(CF)2-β and DPP-(CF)2-γ exhibit a similar way of packing, a small increment in the π-π-stacking distance (0.006 Å) and twist conformation of the grafted electron-donating moieties of DPP-(CF)2-γ are found to reduce its hole mobility.Entities:
Keywords: diketopyrrolopyrrole; optical and electrical properties; organic electronics; polymorphism; π−π stacking
Year: 2016 PMID: 27434658 DOI: 10.1021/acsami.6b05084
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229